A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692747



Internal ID15082713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42678701..42731284hg38UCSC Ensembl
Innerchr15:42970899..43023482hg19UCSC Ensembl
Innerchr15:40758191..40810774hg18UCSC Ensembl
Innerchr15:40758191..40810774hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3852584
hg1952584
hg1852584
hg1752584
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517553
Supporting Variants
Samples
Known GenesCDAN1, STARD9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692747
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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